FDA UDI Not in Commercial Distribution 🇺🇸 United States

Osseofix +

DI: 00844856032231 · Model: 21390 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Osseofix +
Primary DI
00844856032231
Version / Model
21390
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-28
Public Version
4
Public Version Date
2023-04-24
Public Version Status
Update
Public Device Record Key
72c3420a-6cff-4436-8501-924fc18c0c78
Distribution End Date
2023-04-21

Device Description

Osseofix + Radiopaque Cement

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
NDN CEMENT, BONE, VERTEBROPLASTY

GMDN Terms

Code Name
60505 Vertebral bone filler, non-bioabsorbable

Identifiers

Type ID
Primary 00844856032231

Customer Contacts